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Nick M. Marinov

Researcher at Lawrence Livermore National Laboratory

Publications -  23
Citations -  3621

Nick M. Marinov is an academic researcher from Lawrence Livermore National Laboratory. The author has contributed to research in topics: Combustion & NOx. The author has an hindex of 16, co-authored 23 publications receiving 3420 citations. Previous affiliations of Nick M. Marinov include University of Washington.

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A detailed chemical kinetic model for high temperature ethanol oxidation

TL;DR: A detailed chemical kinetic model for ethanol oxidation has been developed and validated against a variety of experimental data sets as discussed by the authors, and good agreement was found in modeling of the data sets obtained from the five different experimental systems.
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Aromatic and Polycyclic Aromatic Hydrocarbon Formation in a Laminar Premixed n-Butane Flame

TL;DR: In this paper, an experimental and detailed chemical kinetic modeling work has been performed to investigate aromatic and polycyclic aromatic hydrocarbons (PAH) formation pathways in a premixed, rich, sooting, n-butane-oxygen-argon burner stabilized flame.
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Modeling of Aromatic and Polycyclic Aromatic Hydrocarbon Formation in Premixed Methane and Ethane Flames

TL;DR: In this paper, a detailed chemical kinetic modeling has been performed to investigate aromatic and polyaromatic hydrocarbon formation pathways in rich, sooting, methane and ethane premixed flames.

Wide range modeling study of dimethyl ether oxidation

TL;DR: A detailed chemical kinetic model has been used to study dimethyl ether (DME) oxidation over a wide range of conditions, such as jet-stirred reactor (JSR) at I and 10 atm, 0.2 < 0 < 2.5, and 800 < T < 1300 K.
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Reaction mechanisms in aromatic hydrocarbon formation involving the C5H5 cyclopentadienyl moiety

TL;DR: In this article, the quantum chemical BAC-MP4 and BACMP2 methods have been used to investigate the reaction mechanisms leading to polycyclic aromatic hydrocarbon (PAH) ring formation, in particular the elementary reaction steps in the conversion of two cyclopentadienyl radicals to naphthalene.